Novel feature of Mycobacterium avium subsp. paratuberculosis, highlighted by characterization of the heparin-binding hemagglutinin adhesin

Louise Lefrançois (1, 2) , Christelle Richer (1) , Thierry Cochard (1) , Sylvie Canepa (3, 4) , Dominique Raze (5, 5) , Philippe Lanotte (6) , Iker A. Sevilla (7) , Karen Stevenson (8) , Marcel A. Behr (9) , Camille Locht (5, 5) , Franck Biet (1)

1 UMR ISP - Infectiologie et Santé Publique
2 McGill University = Université McGill [Montréal, Canada]
3 PRC - Physiologie de la reproduction et des comportements [Nouzilly]
4 Plate-forme d'Analyse Intégrative des Biomolécules
5 CIIL - Centre d’Infection et d’Immunité de Lille - INSERM U 1019 - UMR 9017 - UMR 8204
6 Service Bactériologie-Virologie
7 Departamento de Sanidad Animal
8 MRI - Moredun Research Institute [Penicuik, UK]
9 Département de Médecine

Mycobacterium avium subsp. paratuberculosis comprises two genotypically defined groups, known as the cattle (C) and sheep (S) groups. Recent studies have reported phenotypic differences between M. avium subsp. paratuberculosis groups C and S, including growth rates, infectivity for macrophages, and iron metabolism. In this study, we investigated the genotypes and biological properties of the virulence factor heparin-binding hemagglutinin adhesin (HBHA) for both groups. In Mycobacterium tuberculosis, HBHA is a major adhesin involved in mycobacterium-host interactions and extrapulmonary dissemination of infection. To investigate HBHA in M. avium subsp. paratuberculosis, we studied hbhA polymorphisms by fragment analysis using the GeneMapper technology across a large collection of isolates genotyped by mycobacterial interspersed repetitive-unit-variable-number tandem-repeat (MIRU-VNTR) and IS900 restriction fragment length polymorphism (RFLP-IS900) analyses. Furthermore, we analyzed the structure-function relationships of recombinant HBHA proteins of types C and S by heparin-Sepharose chromatography and surface plasmon resonance (SPR) analyses. In silico analysis revealed two forms of HBHA, corresponding to the prototype genomes for the C and S types of M. avium subsp. paratuberculosis. This observation was confirmed using GeneMapper on 85 M. avium subsp. paratuberculosis strains, including 67 strains of type C and 18 strains of type S. We found that HBHAs from all type C strains contain a short C-terminal domain, while those of type S present a long C-terminal domain, similar to that produced by Mycobacterium avium subsp. avium. The purification of recombinant HBHA from M. avium subsp. paratuberculosis of both types by heparin-Sepharose chromatography highlighted a correlation between their affinities for heparin and the lengths of their C-terminal domains, which was confirmed by SPR analysis. Thus, types C and S of M. avium subsp. paratuberculosis may be distinguished by the types of HBHA they produce, which differ in size and adherence properties, thereby providing new evidence that strengthens the genotypic differences between the C and S types of M. avium subsp. paratuberculosis.

Domaines: Sciences du Vivant [q-bio]

Louise Lefrançois, Christelle Richer, Thierry Cochard, Sylvie Canepa, Dominique Raze, et al.. Novel feature of Mycobacterium avium subsp. paratuberculosis, highlighted by characterization of the heparin-binding hemagglutinin adhesin. Journal of Bacteriology, 2013, 195 (21), pp.4844-4853. ⟨10.1128/JB.00671-13⟩. ⟨hal-01129782⟩